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Epidemiology of herpes zoster and its relationship to varicella in Japan: A 10-year survey of 48,388 herpes zoster cases in Miyazaki prefecture

Journal of medical virology, 2009-12, Vol.81 (12), p.2053-2058

2009

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Reactions in liquid ammonia. 3. Complete aminoethylation of thiol groups in peptides and proteins by ethylenimmine in liquid ammonia

The Journal of biological chemistry, 1972-09, Vol.247 (17), p.5646-5647

1972

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Stoichiometry of the interaction of human plasma alpha 1-proteinase inhibitor with subtilisin BPN

Journal of biochemistry (Tokyo), 1989-01, Vol.105 (1), p.66-71

1989

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Studies of Peptide Antibiotics. XX. Synthesis of Tyrocidine B

Bulletin of the Chemical Society of Japan, 1970, Vol.43 (7), p.2199-2204

1970

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Stoichiometry of the interaction of human plasma alpha sub(1)-proteinase inhibitor with subtilisin BPN

Journal of biochemistry (Tokyo), 1989-01, Vol.105 (1), p.66-71

1989

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Trypsin reactive site of the Vicia angustifolia proteinase inhibitor [broad beans]

Journal of biochemistry (Tokyo), 1978-06, Vol.83 (6), p.1749-1756

1978

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Synthesis of tyrocidine B

Experientia, 1970-06, Vol.26 (6), p.587-588

1970

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Isolation and activities of the trypsin-modified vicia angustifolia proteinase inhibitor lacking carboxyl-terminal hexapeptide

BBA - Enzymology, 1979-01, Vol.568 (1), p.71-79

1979

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Studies of Peptide Antibiotics. XV. The Synthesis of cyclo-(L-Valyl-L-ornithyl-L-leueyl-D-phenylalanyl-L-prolyl-glycyl-glycyl)

Bulletin of the Chemical Society of Japan, 1970, Vol.43 (3), p.914-917

1970

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Location of the disulfide bonds in the antitumor protein neocarzinostatin

Archives of biochemistry and biophysics, 1991-05, Vol.286 (2), p.569-573

1991

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Stoichiometry of the Interaction of Human Plasma α1 -Proteinase Inhibitor with Subtilisin BPN

Journal of biochemistry (Tokyo), 1989-01, Vol.105 (1), p.66-71

1989

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Crystal structure of apo‐neocarzinostatin at 0.15‐nm resolution

European journal of biochemistry, 1993, Vol.213 (2), p.737-741

1993

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Fluorescence labeling of a single sulfhydryl group in human plasma alpha 1-proteinase inhibitor and characterization of the labeled inhibitor

Journal of biochemistry (Tokyo), 1986-09, Vol.100 (3), p.563-570

1986

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Reexamination of the primary structure of an antitumor protein, neocarzinostatin

Archives of biochemistry and biophysics, 1986-04, Vol.246 (1), p.199-205

1986

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Distribution of substance K (neurokinin A) in the brain and peripheral tissues of rats

Brain research, 1986-03, Vol.369 (1), p.400-404

1986

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Fluorescence labeling of a single sulfhydryl group in human plasma alpha sub(1)-proteinase inhibitor and characterization of the labeled inhibitor

Journal of biochemistry (Tokyo), 1986-01, Vol.100 (3), p.563-570

1986

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Removal of the N alpha-benzyloxycarbonyl group from cysteine-containing peptides by catalytic hydrogenolysis in liquid ammonia, exemplified by a synthesis of oxytocin

Journal of the American Chemical Society, 1974-07, Vol.96 (15), p.4978-4981

1974

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New fluorogenic substrate for esterase activity of α-chymotrypsin and related enzymes

Analytical biochemistry, 1985-01, Vol.151 (2), p.534-539

1985

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Rapid and large-scale purification and characterization of renin from mouse submaxillary gland

Archives of biochemistry and biophysics, 1982-09, Vol.217 (2), p.574-581

1982

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Synthesis of thyrocidine C

Tetrahedron letters, 1970-04 (17), p.1471-1472

1970

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Fluorescence Labeling of a Single Sulfhydryl Group in Human Plasma α1-Proteinase Inhibitor and Characterization of the Labeled Inhibitor

Journal of biochemistry (Tokyo), 1986, Vol.100 (3), p.563-570

1986

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Spontaneous deamidation of a protein antibiotic, neocarzinostatin, at weakly acidic pH. Conversion to a homologous inactive preneocarzinostatin due to change of asparagine 83 to aspartic acid 83 accompanied by conformational and biological alterations

Journal of biochemistry (Tokyo), 1977-01, Vol.81 (1), p.25

1977

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Highly sensitive method for determination of esterase activity of α-chymotrypsin and α-chymotrypsin-like enzymes using micro high-performance liquid chromatography

Journal of Chromatography A, 1983-01, Vol.267 (1), p.199-208

1983

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Primary Structure of Neocarzinostatin, an Antitumor Protein

Science (American Association for the Advancement of Science), 1972-11, Vol.178 (4063), p.875-876

1972

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Catalytic hydrogenolysis in liquid ammonia: stability and cleavage of some protecting groups used in peptide synthesis

Tetrahedron letters, 1974, Vol.15 (37), p.3259-3262

1974

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Epidemiology of herpes zoster and its relationship to varicella in Japan: A 10-year survey of 48,388 herpes zoster cases in Miyazaki prefecture

Reactions in liquid ammonia. 3. Complete aminoethylation of thiol groups in peptides and proteins by ethylenimmine in liquid ammonia

Stoichiometry of the interaction of human plasma alpha 1-proteinase inhibitor with subtilisin BPN

Studies of Peptide Antibiotics. XX. Synthesis of Tyrocidine B

Stoichiometry of the interaction of human plasma alpha sub(1)-proteinase inhibitor with subtilisin BPN

Trypsin reactive site of the Vicia angustifolia proteinase inhibitor [broad beans]

Synthesis of tyrocidine B

Isolation and activities of the trypsin-modified vicia angustifolia proteinase inhibitor lacking carboxyl-terminal hexapeptide

Studies of Peptide Antibiotics. XV. The Synthesis of cyclo-(L-Valyl-L-ornithyl-L-leueyl-D-phenylalanyl-L-prolyl-glycyl-glycyl)

Location of the disulfide bonds in the antitumor protein neocarzinostatin

Stoichiometry of the Interaction of Human Plasma α1 -Proteinase Inhibitor with Subtilisin BPN

Crystal structure of apo‐neocarzinostatin at 0.15‐nm resolution

Fluorescence labeling of a single sulfhydryl group in human plasma alpha 1-proteinase inhibitor and characterization of the labeled inhibitor

Reexamination of the primary structure of an antitumor protein, neocarzinostatin

Distribution of substance K (neurokinin A) in the brain and peripheral tissues of rats

Fluorescence labeling of a single sulfhydryl group in human plasma alpha sub(1)-proteinase inhibitor and characterization of the labeled inhibitor

Removal of the N alpha-benzyloxycarbonyl group from cysteine-containing peptides by catalytic hydrogenolysis in liquid ammonia, exemplified by a synthesis of oxytocin

New fluorogenic substrate for esterase activity of α-chymotrypsin and related enzymes

Rapid and large-scale purification and characterization of renin from mouse submaxillary gland

Synthesis of thyrocidine C

Fluorescence Labeling of a Single Sulfhydryl Group in Human Plasma α1-Proteinase Inhibitor and Characterization of the Labeled Inhibitor

Spontaneous deamidation of a protein antibiotic, neocarzinostatin, at weakly acidic pH. Conversion to a homologous inactive preneocarzinostatin due to change of asparagine 83 to aspartic acid 83 accompanied by conformational and biological alterations

Highly sensitive method for determination of esterase activity of α-chymotrypsin and α-chymotrypsin-like enzymes using micro high-performance liquid chromatography

Primary Structure of Neocarzinostatin, an Antitumor Protein

Catalytic hydrogenolysis in liquid ammonia: stability and cleavage of some protecting groups used in peptide synthesis

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